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Saline + Ketamine

Ullevaal University Hospital · FDA-approved active Small molecule

Ketamine blocks NMDA glutamate receptors in the central nervous system, producing rapid-onset dissociative anesthesia and analgesia when administered intravenously in saline solution.

Ketamine blocks NMDA glutamate receptors in the central nervous system, producing rapid-onset dissociative anesthesia and analgesia when administered intravenously in saline solution. Used for Induction and maintenance of general anesthesia, Acute pain management and analgesia, Sedation in intensive care settings.

At a glance

Generic nameSaline + Ketamine
Also known asPhysiological saline 0.9%, Ketamine, ATC code: N01A X03
SponsorUllevaal University Hospital
Drug classNMDA receptor antagonist / Dissociative anesthetic
TargetNMDA receptor (glutamate-gated ion channel)
ModalitySmall molecule
Therapeutic areaAnesthesia / Pain Management
PhaseFDA-approved

Mechanism of action

Ketamine is a non-competitive antagonist at the N-methyl-D-aspartate (NMDA) receptor, a subtype of glutamate receptor. This blockade interrupts pain signal transmission and produces dissociative anesthesia characterized by analgesia, amnesia, and preserved airway reflexes. The saline vehicle is a physiologic carrier for intravenous administration.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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